Related skills
r leadership sas cdisc sdtm📋 Description
- Lead programming strategy across multiple studies and programs.
- Oversee internal programmers and CRO partners.
- Establish and maintain programming standards and processes.
- Manage timelines and resourcing for all programming activities.
- Ensure high-quality deliverables for regulatory submissions.
- Drive adoption of modern programming tools and workflows.
🎯 Requirements
- SAS and/or R expertise; CDISC SDTM/ADaM knowledge.
- Regulatory submissions experience (FDA/EMA/PMDA).
- 8–12+ years of clinical programming in pharma/CRO.
- Lead internal programmers and external vendors.
- Establish programming standards, processes, and best practices.
- Strong communication, leadership, and PM skills.
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